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4LO0

Apo HA17-HA33

Summary for 4LO0
Entry DOI10.2210/pdb4lo0/pdb
Related4LO1 4LO2 4LO3 4LO4 4LO5 4LO6 4LO7 4LO8
DescriptorHA-33, HA-17 (3 entities in total)
Functional Keywordsprogenitor toxin complex, botulinum neurotoxin, botulism, neurotoxin associated protein, hemagglutinin, carbohydrate/sugar binding, secreted protein, protein transport
Biological sourceClostridium botulinum
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Total number of polymer chains3
Total formula weight85232.51
Authors
Lee, K.,Gu, S.,Jin, L.,Le, T.T.,Cheng, L.W.,Strotmeier, J.,Kruel, A.M.,Yao, G.,Perry, K.,Rummel, A.,Jin, R. (deposition date: 2013-07-12, release date: 2013-10-30, Last modification date: 2024-02-28)
Primary citationLee, K.,Gu, S.,Jin, L.,Le, T.T.,Cheng, L.W.,Strotmeier, J.,Kruel, A.M.,Yao, G.,Perry, K.,Rummel, A.,Jin, R.
Structure of a Bimodular Botulinum Neurotoxin Complex Provides Insights into Its Oral Toxicity.
Plos Pathog., 9:e1003690-e1003690, 2013
Cited by
PubMed Abstract: Botulinum neurotoxins (BoNTs) are produced by Clostridium botulinum and cause the fatal disease botulism, a flaccid paralysis of the muscle. BoNTs are released together with several auxiliary proteins as progenitor toxin complexes (PTCs) to become highly potent oral poisons. Here, we report the structure of a ∼760 kDa 14-subunit large PTC of serotype A (L-PTC/A) and reveal insight into its absorption mechanism. Using a combination of X-ray crystallography, electron microscopy, and functional studies, we found that L-PTC/A consists of two structurally and functionally independent sub-complexes. A hetero-dimeric 290 kDa complex protects BoNT, while a hetero-dodecameric 470 kDa complex facilitates its absorption in the harsh environment of the gastrointestinal tract. BoNT absorption is mediated by nine glycan-binding sites on the dodecameric sub-complex that forms multivalent interactions with carbohydrate receptors on intestinal epithelial cells. We identified monosaccharides that blocked oral BoNT intoxication in mice, which suggests a new strategy for the development of preventive countermeasures for BoNTs based on carbohydrate receptor mimicry.
PubMed: 24130488
DOI: 10.1371/journal.ppat.1003690
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.055 Å)
Structure validation

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數據於2024-11-06公開中

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